chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142575581142575582GA20GENIChomozygous61902435
1142576026142576027CT23GENIChomozygous61902437
1142576040142576041GA20GENIChomozygous61902438
1142576052142576053TC21GENIChomozygous61531037
1142576697142576698CT26GENIChomozygous61902439
1142576902142576903CA25GENIChomozygous61902440
1142577646142577647TA28GENIChomozygous61902441
1142577902142577912TGTGTGTGTG----------5GENICheterozygous62246583
1142577908142577912TGTG----5GENICheterozygous62162131
1142578205142578206CT25GENIChomozygous61531048
1142578951142578952A-16GENICheterozygous62246584
1142579734142579735GA41GENIChomozygous61902442
1142582435142582436GA29GENIChomozygous61902443
1142583394142583395TA29GENIChomozygous61902444
1142583893142583894TC33GENIChomozygous61531068
1142584110142584111GA34GENIChomozygous61902445
1142584811142584812GA21GENIChomozygous61902446
1142585462142585463TC22GENIChomozygous61531070
1142587717142587718AAAC4GENIChomozygous62162133
1142591967142591968CT24GENIChomozygous60876195
1142594258142594259AG16GENIChomozygous61902447
1142594447142594448TTG15GENICheterozygous62162137
1142600162142600163TTC11GENIChomozygous62162139
1142600163142600164TTTTTTTTTCGGAGCTGGGGAC11GENIChomozygous62162141
1142600619142600620GGGGTT9GENIChomozygous62162143
1142600657142600658AAG10GENIChomozygous62162145
1142600658142600659CCTCAGT10GENIChomozygous62162147
1142600660142600661GGTAGAGCGCTTGCCTAGC9GENIChomozygous62162149
1142600663142600664GGCA9GENIChomozygous61765877
1142600693142600703AAAAAAAAAA----------5GENIChomozygous60876200
1142602001142602002T-3GENICheterozygous60876202
1142614102142614103CA35GENIChomozygous60876204
1142614225142614226GA15GENIChomozygous62162151